Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Geminiganesan, Sangeetha"'
Autor:
Geminiganesan, Sangeetha1 sangeethaperungo@gmail.com, Kumar, Ashwin Raj2, Kumaravel, S.3, Priya, C. D. Mohana4, Arunaa, Sathyamurthy5, Babu, Ramesh5
Publikováno v:
Journal of Indian Association of Pediatric Surgeons. Mar/Apr2024, Vol. 29 Issue 2, p104-109. 6p.
Autor:
Geminiganesan Sangeetha, Ramesh Babu
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 28, Iss 4, Pp 278-281 (2023)
Background and Aims: In this cost-effectiveness model, we compared the cost-effectiveness of commonly used urinary biomarkers with conventional diuretic renogram (DR) in diagnosing ureteropelvic junction obstruction (UPJO). We hypothesized that urina
Externí odkaz:
https://doaj.org/article/e06d7cafac5646aebb018dcbc75345e6
Akademický článek
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Publikováno v:
BMJ Case Rep
Juvenile dermatomyositis (JDM) is the most common inflammatory myopathy in children and is characterised by the presence of proximal muscle weakness, heliotrope dermatitis, Gottron’s papules and occasionally auto antibodies. The disease primarily a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a798058eb9ad4555d9047dd7b7b8c389
https://pubmed.ncbi.nlm.nih.gov/33795282
https://pubmed.ncbi.nlm.nih.gov/33795282
Autor:
Geminiganesan Sangeetha, Ramesh Babu
Publikováno v:
Pediatric Nephrology. 37:2277-2287
Multiple urinary biomarkers have been reported in differentiation of nonobstructive dilatation (NOD) from ureteropelvic junction obstruction (UPJO). In this meta-analysis, we compared the accuracy of common urinary biomarkers applicable to UPJO. A sy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::429db4f85eea4a6cfe2e9742408e59e5
https://doi.org/10.1007/s00467-022-05488-3
https://doi.org/10.1007/s00467-022-05488-3
Publikováno v:
BMJ Case Rep
Alkaptonuria is a rare genetic disorder resulting in abnormality of tyrosine metabolism. It is one of the Garrod’s tetrad of ‘inborn errors of metabolism’ proposed to have Mendelian recessive inheritance. The disorder is characterised by deposi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7441fce7c0aadfe8d88fcca9dee07366
https://pubmed.ncbi.nlm.nih.gov/33541951
https://pubmed.ncbi.nlm.nih.gov/33541951
Autor:
Geminiganesan, Sangeetha, Ramanan, Padmasani Venkat, J., Dhivyalakshmi, Harshita, Bhogavalli Lakshmi, Sriram, Deepalakshmi
Publikováno v:
EJIFCC
Holoprosencephaly is a developmental abnormality caused due to incomplete cleavage of the rostral neural tube (basal forebrain) structures during early embryogenesis. This defect causes incomplete separation of the right and left cerebral hemispheres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b83612813ad65cca8924fe073816786e
http://europepmc.org/articles/PMC8751397
http://europepmc.org/articles/PMC8751397
Autor:
Geminiganesan, Sangeetha, Ganesan, Swathi, Jayaraj, Jaippreetha, Barathi, G, Muthu Kumar, S, Samy, Nandha K
Publikováno v:
EJIFCC
CASE REPORT Recent advances in genomics have uncovered the molecular mechanisms involved in the broad spectrum of variation associated with steroid-resistant nephrotic syndrome. Over 50 monogenic causes of steroid-resistant nephrotic syndrome have be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::68f269a5811ef3f3e3cf4decbdca96a7
http://europepmc.org/articles/PMC8592633
http://europepmc.org/articles/PMC8592633
Autor:
Geminiganesan, Sangeetha1 sangeethaperungo@gmail.com, Ravichandran, Latha2, Srinivasan, Ramesh Babu3
Publikováno v:
Sri Ramachandra Journal of Health Sciences. Jul-Dec2022, Vol. 1 Issue 1, p31-33. 3p.
Akademický článek
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